Zobrazeno 1 - 10
of 120
pro vyhledávání: '"a1166c polymorphism"'
Autor:
Pidruchna Svitlana, Shmanko Volodymyr, Zakharchuk Uliana, Tokarskyy Oleksandr, Hnizdyukh Roman, Lynkhatskyi Petro, Kuzmak Iryna, Yaroshenko Tetyana, Bandas Iryna, Vasylyshyn Nadija, Ostrivka Oksana, Mudra Alla, Palytsya Liliya, Letniak Nataliya, Pohorielova Oksana
Publikováno v:
Endocrine Regulations, Vol 58, Iss 1, Pp 153-157 (2024)
Objective. Genetic factors substantially contribute to the development and duration of arterial hypertension. The study of the A1166C polymorphism of the angiotensin II type 1 receptor gene (AGTR1) in arterial hypertension is an auspicious area for a
Externí odkaz:
https://doaj.org/article/254690d6c5974d0f9bafe79216006842
Autor:
T.V. Kolesnyk, O.V. Fursa
Publikováno v:
Medičnì Perspektivi, Vol 27, Iss 3, Pp 56-64 (2022)
The article presents the results of a study of the daily blood pressure profile, taking into account the polymorphism of the angiotensin II type 1 receptor gene in patients with arterial hypertension with past myocardial infarction. The study involve
Externí odkaz:
https://doaj.org/article/ab09d36578b3431490bcc14a3271957f
Akademický článek
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Publikováno v:
Middle East Journal of Digestive Diseases, Vol 10, Iss 2, Pp 96-104 (2018)
BACKGROUND Genetic predisposition may have important role in pathogenesis of non-alcoholic fatty liver disease (NAFLD). Angiotensin II type I receptor (AGTR1) has been known to involve in the process of liver steatosis and fibrosis. This study aimed
Externí odkaz:
https://doaj.org/article/0959dd095e9e4905b54f51340aacb85f
Publikováno v:
The Egyptian Heart Journal, Vol 68, Iss 3, Pp 165-169 (2016)
The pathogenesis of essential hypertension (EH) is affected by genetic and environmental factors. Mutations in hypertension-related genes can affect blood pressure (BP) via alteration of salt and water reabsorption by the nephron. The genes of the re
Externí odkaz:
https://doaj.org/article/0855ed229a7e4719b417e4d6e8abdbb4
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 12, Iss 3, Pp 331-336 (2016)
Atrial fibrillation (AF) is the most common heart rhythm disturbance. It is believed that the primary form of AF is genetically determined in most cases, but the genetic component cannot be excluded in the secondary form of AF. AF is a heterogeneous
Externí odkaz:
https://doaj.org/article/97dbcf2b34114fe5b1eccaeab11ed76b
Publikováno v:
Journal of Nephropathology, Vol 4, Iss 3, Pp 69-76 (2015)
Background: There are inconsistent reports related to the role of angiotensin II type 1 receptor (AT1R) on the risk of type 2 diabetes mellitus (T2DM) and its renal complications. Objectives: To identify the association between AT1R A1166C variants w
Externí odkaz:
https://doaj.org/article/7b99c398ff444adc8f8832ecf85904fc
Autor:
Avshesh Mishra, Anshika Srivastava, Surendra Kumar, Tulika Mittal, Naveen Garg, Surendra Kumar Agarwal, Shantanu Pande, Balraj Mittal
Publikováno v:
Indian Heart Journal, Vol 67, Iss 3, Pp 214-221 (2015)
Background: Left ventricular dysfunction (LVD) with subsequent congestive heart failure (CHF) constitutes the final common pathway for a host of cardiac disorders. The impaired LV function develops in response to an ischemic insult followed by a fall
Externí odkaz:
https://doaj.org/article/866f7494bcf744c5b1bc458ba930ea90
Autor:
Kolesnyk T.V., Fursa O.V.
Publikováno v:
Medicni perspektivi; Vol. 27 No. 3 (2022); 56-64
Медичні перспективи; Том 27 № 3 (2022); 56-64
Медичні перспективи; Том 27 № 3 (2022); 56-64
The article presents the results of a study of the daily blood pressure profile, taking into account the polymorphism of the angiotensin II type 1 receptor gene in patients with arterial hypertension with past myocardial infarction. The study involve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9891a5a164b3fda9dadd1704ceaff309
https://zenodo.org/record/7257544
https://zenodo.org/record/7257544
Publikováno v:
Терапевтический архив, Vol 0, Iss 1, Pp 64-69 (2009)
Aim. To study distribution of the incidence of polymorphic markers of the genes ACE (I/D), ANG (M235T), AT1R (A1166C), CYP11B2 (T344C) in patients with essential hypertension (EH) of Uzbek nationality; to determine carriage of gene combinations with
Externí odkaz:
https://doaj.org/article/7310f4a3c947485abdcf1b6b92ad5917